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Ingo Mellinghoff

· Professor

Cornell University · Pharmacology and Chemical Biology

Active 1991–2026

h-index105
Citations45.0k
Papers597357 last 5y
Funding$6.7M

Academic metrics are sourced from OpenAlex and public funding records; values may differ from Google Scholar.

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About

Ingo Mellinghoff, MD, FACP, is a physician-scientist whose laboratory focuses on the study of molecular pathways that regulate brain tumor growth. His long-term goal is to develop therapeutic paradigms that target specific properties of primary brain tumors, including genetic alterations in cancer signaling pathways, unique aspects of brain tumor metabolism, and interactions of brain tumor cells with their brain microenvironment. His research involves studies in experimental brain tumor models that are closely linked to the evaluation of novel agents in early-phase clinical trials. Dr. Mellinghoff has contributed to significant advancements in the treatment of low-grade gliomas, including the development and clinical testing of targeted drugs such as vorasidenib and ivosidenib, which reduce tumor-associated metabolites and show encouraging tumor responses. His work has led to the FDA approval of drugs for low-grade glioma with IDH gene mutations and has been published in high-impact journals. His research also explores the use of liquid biopsies from spinal fluid to guide brain tumor diagnosis and treatment, and he has been involved in studies tracking tumor evolution through cerebrospinal fluid analysis.

Research topics

  • Internal medicine
  • Oncology
  • Medicine
  • Cancer research
  • Pathology
  • Biology
  • Engineering
  • Genetics
  • Intensive care medicine
  • Medical physics

Selected publications

  • Glioblastoma and Other Primary Brain Malignancies in Adults

    JAMA · 2023 · 1129 citations

    Senior authorCorresponding

    Importance: Malignant primary brain tumors cause more than 15 000 deaths per year in the United States. The annual incidence of primary malignant brain tumors is approximately 7 per 100 000 individuals and increases with age. Five-year survival is approximately 36%. Observations: Approximately 49% of malignant brain tumors are glioblastomas, and 30% are diffusely infiltrating lower-grade gliomas. Other malignant brain tumors include primary central nervous system (CNS) lymphoma (7%) and malignan…

  • Glioblastoma in adults: a Society for Neuro-Oncology (SNO) and European Society of Neuro-Oncology (EANO) consensus review on current management and future directions

    Neuro-Oncology · 2020 · 1111 citations

    Glioblastomas are the most common form of malignant primary brain tumor and an important cause of morbidity and mortality. In recent years there have been important advances in understanding the molecular pathogenesis and biology of these tumors, but this has not translated into significantly improved outcomes for patients. In this consensus review from the Society for Neuro-Oncology (SNO) and the European Association of Neuro-Oncology (EANO), the current management of isocitrate dehydrogenase w…

  • Vorasidenib in IDH1- or IDH2-Mutant Low-Grade Glioma

    New England Journal of Medicine · 2023 · 683 citations

    1st authorCorresponding

    BACKGROUND: Isocitrate dehydrogenase (IDH)-mutant grade 2 gliomas are malignant brain tumors that cause considerable disability and premature death. Vorasidenib, an oral brain-penetrant inhibitor of mutant IDH1 and IDH2 enzymes, showed preliminary activity in IDH-mutant gliomas. METHODS: In a double-blind, phase 3 trial, we randomly assigned patients with residual or recurrent grade 2 IDH-mutant glioma who had undergone no previous treatment other than surgery to receive either oral vorasidenib…

  • Inaugural Results of the Individualized Screening Trial of Innovative Glioblastoma Therapy: A Phase II Platform Trial for Newly Diagnosed Glioblastoma Using Bayesian Adaptive Randomization

    Journal of Clinical Oncology · 2023 · 47 citations

    PURPOSE: The Individualized Screening Trial of Innovative Glioblastoma Therapy (INSIGhT) is a phase II platform trial that uses response adaptive randomization and genomic profiling to efficiently identify novel therapies for phase III testing. Three initial experimental arms (abemaciclib [a cyclin-dependent kinase [CDK]4/6 inhibitor], neratinib [an epidermal growth factor receptor [EGFR]/human epidermal growth factor receptor 2 inhibitor], and CC-115 [a deoxyribonucleic acid-dependent protein k…

  • Hypothetical generalized framework for a new imaging endpoint of therapeutic activity in early phase clinical trials in brain tumors

    Neuro-Oncology · 2022 · 23 citations

    Imaging response assessment is a cornerstone of patient care and drug development in oncology. Clinicians/clinical researchers rely on tumor imaging to estimate the impact of new treatments and guide decision making for patients and candidate therapies. This is important in brain cancer, where associations between tumor size/growth and emerging neurological deficits are strong. Accurately measuring the impact of a new therapy on tumor growth early in clinical development, where patient numbers a…

Recent grants

Frequent coauthors

  • Patrick Y. Wen

    442 shared
  • Timothy F. Cloughesy

    University of California, Los Angeles

    428 shared
  • Carl Campos

    Memorial Sloan Kettering Cancer Center

    284 shared
  • Michael D. Prados

    University of California, San Francisco

    251 shared
  • Lisa M. DeAngelis

    Memorial Sloan Kettering Cancer Center

    241 shared
  • Paul S. Mischel

    Stanford University

    205 shared
  • Cameron Brennan

    172 shared
  • John G. Kuhn

    University of California, Los Angeles

    172 shared

Labs

  • The Ingo Mellinghoff LabPI

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